vigilance reporting

  • ANVISA Notivisa Vigilance SOP + Reportability Worksheet — RDC 67/2009 (Brazil)

    ANVISA Notivisa Vigilance SOP + Reportability Worksheet — RDC 67/2009 (Brazil)

    69.00

    Process Package — Vigilance Reporting Brazil (Notivisa) Complete framework for Brazilian medical device vigilance. Covers RDC 67/2009 reportability assessment, Notivisa submission, causality classification, foreign event tracking, and field actions. What’s included: SOP-VIG-BR Vigilance Reporting Brazil — full procedure with the 4-question reportability framework per RDC 67/2009, Notivisa submission process, causality classification, timelines (10 days for…

  • FDA MDR SOP + Reportability Worksheet — 21 CFR Part 803 (USA)

    FDA MDR SOP + Reportability Worksheet — 21 CFR Part 803 (USA)

    69.00

    Process Package — Vigilance Reporting USA (FDA MDR) Complete framework for FDA Medical Device Reporting under 21 CFR Part 803. Covers MDR reportability (death/serious injury caused or contributed to, plus the unique ‘malfunction recurrence’ criterion), 30-day standard timeline vs 5-day expedited reporting, eMDR submission via the FDA Electronic Submissions Gateway, and the §803.18 records retention…

  • Health Canada MPR + Foreign Risk Notification SOP — SOR/98-282 §59 & §61.2

    Health Canada MPR + Foreign Risk Notification SOP — SOR/98-282 §59 & §61.2

    69.00

    Process Package — Vigilance Reporting Canada Canada has TWO distinct reporting paths and both are audited. (1) MPR — Mandatory Problem Report under SOR/98-282 §59 with 10-day or 30-day timelines for events in Canada; (2) FRN — Foreign Risk Notification under §61.2 requiring 72-hour notification when a foreign regulator/manufacturer has taken corrective action abroad on…

  • PMDA Registration SOP + JMDN Template — Shonin / Ninsho / Todokede (Japan)

    PMDA Registration SOP + JMDN Template — Shonin / Ninsho / Todokede (Japan)

    69.00

    Process Package — Vigilance Reporting Japan (PMDA) Complete framework for Japanese medical device vigilance under PMD Act Art. 68-10. Covers the LISTED vs UNLISTED logic (events already in tempu bunsho follow 30-day path; UNLISTED follow stricter 15-day path), causality assessment, mandatory PSB/PSD fax notification for deaths, and tempu bunsho management strategy. What’s included: SOP-VIG-JP Vigilance…

  • TGA MDIR SOP + Exemption Worksheet — Australia

    TGA MDIR SOP + Exemption Worksheet — Australia

    69.00

    Process Package — Vigilance Reporting Australia (TGA) Complete framework for Australian medical device incident reporting. Covers Medical Device Incident Report (MDIR) under TG (MD) Regulations 2002, the Australia-specific exemption mechanism (events that meet specific criteria can be aggregated in Annual Reports rather than reported individually), and the PRAC (Procedure for Recalls, Product Alerts and Product…